Atomistic mechanisms of water vapor-induced surface passivation.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37910618.
- Also identified by DOI 10.1126/sciadv.adh5565 and PMC identifier 10619940.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The microscopic mechanisms underpinning the spontaneous surface passivation of metals from ubiquitous water have remained largely elusive. Here, using in situ environmental electron microscopy to atomically monitor the reaction dynamics between aluminum surfaces and water vapor, we provide direct experimental evidence that the surface passivation results in a bilayer oxide film consisting of a crystalline-like Al(OH)<sub>3</sub> top layer and an inner layer of amorphous Al<sub>2</sub>O<sub>3</sub>. The Al(OH)<sub>3</sub> layer maintains a constant thickness of ~5.0 Å, while the inner Al<sub>2</sub>O<sub>3</sub> layer grows at the Al<sub>2</sub>O<sub>3</sub>/Al interface to a limiting thickness. On the basis of experimental data and atomistic modeling, we show the tunability of the dissociation pathways of H<sub>2</sub>O molecules with the Al, Al<sub>2</sub>O<sub>3</sub>, and Al(OH)<sub>3</sub> surface terminations. The fundamental insights may have practical significance for the design of materials and reactions for two seemingly disparate but fundamentally related disciplines of surface passivation and catalytic H<sub>2</sub> production from water.